ProfileGDS1065 / 213599_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 63% 52% 73% 54% 65% 69% 54% 61% 62% 65% 60% 67% 66% 74% 69% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 175.663
GSM24653Normal subject 245.352
GSM24654Normal subject 315073
GSM24655A3243G-MELAS subject 136.954
GSM24656A3243G-MELAS subject 28565
GSM24657A3243G-MELAS subject 3157.969
GSM24658A3243G-MELAS subject 446.854
GSM24659A3243G-PEO subject 157.261
GSM24660A3243G-PEO subject 264.762
GSM24661A3243G-PEO subject 356.465
GSM24662A3243G-PEO subject 45660
GSM24663mtDNA "Common"-deletion subject 194.267
GSM24664mtDNA "Common"-deletion subject 2153.766
GSM24665mtDNA "Common"-deletion subject 3195.174
GSM24666mtDNA "Common"-deletion subject 4160.969